🏆 Finalist — NIH Data Sharing Index (“S-Index”) Challenge

Lincoln M. P. Shade

University of Kentucky

ORCID: 0000-0001-6093-4823
Biochemistry, Genetics and Molecular BiologyMedicine

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 100%percentile
0Author DataRank

Indexed papers

1in pilot corpus
datarank_citation_only_1hop_v6· scope data_onlyMethodology
Why this DataRank?

An author's DataRank is the sum of the DataRanks of all 1 indexed paper attributed to them. A prolific author with many moderate-impact papers can outrank one with a single high-impact paper.

Author scores recompute whenever paper DataRanks are refreshed, so this number lags the underlying paper scores by at most one batch run.

Read the full methodology →

Papers

Driven by 9 papers. Top paper: “GWAS of multiple neuropathology endophenotypes identifies new risk loci and provides insights into the genetic risk of dementia”.

GWAS of multiple neuropathology endophenotypes identifies new risk loci and provides insights into the genetic risk of dementia

Nature Genetics(2024)10.1038/s41588-024-01939-9
N/A
1.1DataRank · unranked
66 citations

Yuriko Katsumata, Erin L. Abner, Khine Zin Aung, Steven A. Claas, Qi Qiao +91 more

LATE-NC risk alleles (in TMEM106B, GRN, and ABCC9 genes) among persons with African ancestry

Journal of Neuropathology & Experimental Neurology(2023)10.1093/jnen/nlad059
N/A
0.449DataRank · unranked
19 citations

David W. Fardo, Lincoln M. P. Shade, James D. Bowen, Paul K. Crane, Gail P. Jarvik +94 more

Refining CFTR-Related Metabolic Syndrome (CRMS)/Cystic Fibrosis Screen Positive, Inconclusive Diagnosis (CFSPID) Diagnosis: Impact of CFTR2 Variant Classifications

International Journal of Neonatal Screening(2025)10.3390/ijns11030060
N/A
0.165DataRank · unranked
2 citations

Alex Quinn, Lincoln M. P. Shade, Meghan E. McGarry, MacKenzie Wyatt

Genome-wide association study of multiple neuropathology endophenotypes identifies novel risk loci and provides insights into known Alzheimer’s risk loci

medRxiv(2022)10.1101/2022.12.13.22282475
N/A
0DataRank · unranked
1 citations

Yuriko Katsumata, Steven A. Claas, Mark Ebbert, Erin L. Abner, Timothy J. Hohman +9 more

Genetic associations with dementia‐related proteinopathy: Application of item response theory

Alzheimer s & Dementia(2024)10.1002/alz.13741
N/A
0DataRank · unranked
10 citations

David W. Fardo, Lincoln M. P. Shade, Xian Wu, Shama D. Karanth, Timothy J. Hohman +10 more

Brain arteriolosclerosis

Acta Neuropathologica(2020)10.1007/s00401-020-02235-6
N/A
0DataRank · unranked
212 citations

Harry V. Vinters, Seth Love, Donna M. Wilcock, Lea T. Grinberg, Julie A. Schneider +20 more

Whole genome sequence association analysis of brain structural volume measures in the NHLBI TOPMed Program highlights novel loci in diverse participants

10.1101/2025.06.11.25329426
N/A
0DataRank · unranked
0 citations

Mohsen Sharifitabar, Alexa Beiser, Claudia L. Satizábal, Thomas H. Mosley, Joanne E. Curran +34 more

Analysis of genes (TMEM106B, GRN, ABCC9, KCNMB2, and APOE) implicated in risk for LATE-NC and hippocampal sclerosis provides pathogenetic insights: a retrospective genetic association study

Acta Neuropathologica Communications(2021)10.1186/s40478-021-01250-2
N/A
0DataRank · unranked
58 citations

Peter T. Nelson, Yuriko Katsumata, Lincoln M. P. Shade, Kevin L. Boehme, Merilee Teylan +7 more

Multiple gene variants linked to Alzheimer's-type clinical dementia via GWAS are also associated with non-Alzheimer's neuropathologic entities

Neurobiology of Disease(2022)10.1016/j.nbd.2022.105880
N/A
0DataRank · unranked
46 citations

Lincoln M. P. Shade, Timothy J. Hohman, Julie A. Schneider, David A. Bennett, José M. Farfel +4 more